raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:183444

Genetic porokeratosis

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enGenetic porokeratosis
frPorokératose génétique
dePorokeratose, genetisch bedingte
esPoroqueratosis genética
itPorocheratosi genetica
nlGenetische porokeratose
ptPoroqueratose genética
plPorokeratoza uwarunkowana genetycznie
csGeneticky podmíněná porokeratóza
ukГенетично обумовлений порокератоз
zh遗传性汗孔角化症
trGenetik porokeratoz
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5680580Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (3):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card